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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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22q11.2DS
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D004062 |
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catch22
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D004062 |
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autosomal dominant opitz g bbb syndrome
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D004062 |
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VCF syndrome
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D004062 |
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sedlackova syndrome
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D004062 |
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shprintzen syndrome
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D004062 |
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syndrome, DiGeorge
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D004062 |
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syndrome, VCF
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D004062 |
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syndrome, sedlackova
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D004062 |
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syndrome, shprintzen
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D004062 |
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syndrome, velo-cardio-facial
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D004062 |
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syndrome, velocardiofacial
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D004062 |
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deletion syndrome, 22q11.2
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D004062 |
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familial third and fourth pharyngeal pouch syndrome
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D004062 |
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conotruncal anomaly face syndrome (CTAF)
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D004062 |
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